1. Volume 21, Issue 4, Pages 934-942 (October 2017)
Thymospheres Are Formed by Mesenchymal Cells with the Potential to Generate Adipocytes, but Not Epithelial Cells 
Julie M. Sheridan, Ashleigh Keown, Antonia Policheni, Siti N.A. Roesley, Noa Rivlin, Noam Kadouri, Matthew E. Ritchie, Reema Jain, Jakub Abramson, Tracy S.P. Heng, Daniel H.D. Gray 
Cell Reports 
Volume 21, Issue 4, Pages (October 2017)
DOI: /j.celrep
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2. Cell Reports 2017 21, 934-942DOI: (10.1016/j.celrep.2017.09.090)
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3. Figure 1
Two Phenotypically Distinct TSFC Populations in the Adult Thymus
(A) Flow cytometric analysis of EpCAM versus SCA-1 staining on CD45−TER-119−CD31− (Lin−) thymus cells (representative of 10 experiments). See also Figure S1.
(B) Representative image of thymosphere culture derived from Lin−EpCAM−SCA-1+ cells plated at 15,000 cells/mL. Inset: magnified region showing thymospheres with typical morphology. Scale bar, 100 μm.
(C) Flow cytometric analysis of Lin−EpCAM− thymus cells showing SCA-1 versus MTS-15 staining (representative of 7 experiments).
(D) Frequencies of MTS-15+ cells and MTS-15− cells as a percentage of total Lin−EpCAM−SCA-1+ population (mean ± SEM, n = 7 experiments).
(E) Limiting dilution analysis of Lin−EpCAM−SCA-1+ subpopulations. Indicated numbers of cells were plated in thymosphere cultures and maintained for 7 days. Numbers of thymosphere-containing wells at each cell dose was used to calculate TSFC frequency. Estimates of frequency ± 95% confidence intervals are given; data are from 4 experiments (p = 0.703).
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4. Figure 2 TSFCs and Their Thymosphere Progeny Are Not Epithelial
(A) Maximal intensity projection immunofluorescence image of a thymosphere generated from Lin−EpCAM−SCA-1+ cells showing anti-keratin staining (red) counterstained with DAPI (nuclei, blue). Scale bar, 25 μm. Data are representative of 6 independent experiments.
(B) Representative flow cytometric analysis of Lin− thymus cells showing EpCAM versus keratin expression. Numbers indicate the percentage of cells within the respective regions and are representative of greater than 3 samples in 3 independent experiments. See also Figure S2.
(C) Representative immunofluorescence images of flow cytometrically purified Lin−EpCAM+, Lin−EpCAM−MTS-15+, and Lin−EpCAM−MTS-15− subpopulations stained with anti-keratin antibodies (green) and DAPI (nuclei, red). Scale bars, 40 μm. Data are representative of 3 independent experiments.
(D) Frequency (%) of keratin+ cells in individual populations as determined by flow cytometry (black) and immunofluorescence (white) (mean ± SEM; representative of 3 independent experiments).
(E) Flow cytometric analysis of a grafted RTOC generated from E15.5 BALB/c thymus cells (H-2Kb−) spiked with or without thymospheres derived from EpCAM−YFP− cells (H-2Kb+) from Foxn1cre;R26R-EYFP mice. Identification of thymosphere-derived cells in the Lin− compartments using anti-H-2Kb antibody in thymosphere-containing (left, center) and carrier-only graft (right).
(F) Comparison of YFP expression induced by Foxn1cre activity, and EpCAM versus MHC class II expression on carrier (H-2Kb−) and thymocyte-derived (H-2Kb+) cells in a graft (identified with an asterisk [∗] in Table S1).
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5. Figure 3 EpCAM− Cell-Derived Thymospheres Can Incorporate EpCAM+ TECs
(A) Maximal intensity projection image of immunofluorescent staining of thymospheres generated from purified Lin−EpCAM− cells (left) and unfractionated CD45− cells (right) showing nuclei (DAPI, blue) and keratin (red). Data are representative of 6 experiments. Scale bars, 20 μm.
(B) Quantification of keratin+ bodies per thymosphere. 18–24 z stacks were scored per group from 5–6 experiments. Groups were compared using an unpaired t test with Welch’s correction (∗∗∗∗p = < ).
(C) Maximal intensity projection of immunofluorescent staining of a thymosphere generated from wild-type Lin−EpCAM− cells cultured in the presence of YFP+EpCAM+ TECs (DAPI [nuclei], blue; anti-YFP, green). Scale bar, 25 μm.
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6. Figure 4
TSFCs Are Mesenchymal Cells with Adipocyte Differentiation Capacity
(A) Flow cytometric analysis of adult thymus cells from Foxn1cre;R26R-EYFP (top), Wnt1cre;R26R-EYFP (middle) and MesP1cre;R26R-EYFP (bottom) mice showing YFP expression in Lin−EpCAM+ and Lin−EpCAM−SCA-1+ subpopulations. Profiles are representative of 5 individual mice from two experiments.
(B) Frequency (%) of YFP+ cells in Lin−EpCAM+, Lin−EpCAM−SCA-1+, Lin−EpCAM−SCA-1+MTS-15+, and Lin−EpCAM−SCA-1+MTS-15+ populations for indicated Cre recombinase mouse lines crossed with the R26R-EYFP mouse line (mean ± SEM; n = 3–8 mice from 2–4 independent experiments). Control group composed of Foxn1cre+/+; R26RYFP/+, Wnt1cre+/+; R26RYFP/+, and MesP1cre+/+; R26RYFP/+ mice. Lin−EpCAM+: control versus Foxn1cre, p = < ; control versus Wnt1cre, p = 0.48; control versus MesP1cre, p = Lin−EpCAM−SCA-1+: control versus Foxn1cre, p = 0.1; control versus Wnt1cre, p = 0.001; control versus MesP1cre, p = Groups were compared using an unpaired t test with Welch’s correction (∗p ≤ 0.05; ∗∗p = ≤ 0.01; ∗∗∗∗p ≤ ).
(C) Maximal intensity projection images of thymospheres generated from purified Lin−EpCAM−SCA-1+ YFP+ cells from the thymus of 8- to 10-week-old Wnt1cre;R26R-EYFP mice. Data are representative of 3 independent experiments. Scale bar, 25 μm.
(D) Representative images of oil red O immunocytochemistry (left) and immunofluorescent anti-FABP4 (green) and DAPI nuclear counterstain (blue) (right) on Lin−EpCAM−SCA1+ TSFCs cultured for 14 days under maintenance (control) or adipocyte differentiation conditions. Scale bars, 100 μm. Data are representative of 3 independent experiments.
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